UK Group Quality Director Pharmaceutical, Qualified Person/QP
Posted a week ago by Russell Taylor Group Ltd
UK Group Quality Director Pharmaceutical, Qualified Person/QP
Type: Permanent
Location: Onsite, 5 days a week - Cheshire based
Our client, a multi sited pharmaceutical company is looking for an experienced QP /QM/QD to work onsite at their Cheshire site - reporting directly to the MD, the QD will manage the quality function/s / teams for multiple sites within the group. The QD will be responsible for 5 direct & 40+ indirect reports.
The role:
• Manage the Quality Function across business entities ensuring Compliance status is maintained in support of business strategy
• Provide assistance to all functions within the business on technical and regulatory matters to ensure changing regulatory landscapes are accommodated in support of business objectives
• To lead, motivate and develop the quality teams in support of business plans and profitability goals
• Performing duties as required by a Pharmaceutical Qualified Person under pertinent regulations
• Ensure delivery of quality oversight in in-house and external third-party manufacturing operations
• Provide guidance to Sales and Marketing teams engaged in UK and Export territories as appropriate
• Liaise with and undertake the role of principle point of contact for UK MHRA and UK Home Office Departments in support of business strategy
• To promote and adhere to Health, Safety and Environmental regulations to ensure the wellbeing of the company's employees, contractors and visitors in compliance with legislative requirements.
• To act as a pharmaceutical qualified person to certify products as suitable for release to market
The Person:
• QP qualification essential
• Significant experience working as in a senior quality role within solid dose and none - sterile liquid pharmaceutical settings working and implementing QMS strategies.
• Significant experience working with cGxP regulations
• Previous management/ supervisory experience in a quality setting
Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or GDPR please get in touch with us here.
Type: Permanent
Location: Onsite, 5 days a week - Cheshire based
Our client, a multi sited pharmaceutical company is looking for an experienced QP /QM/QD to work onsite at their Cheshire site - reporting directly to the MD, the QD will manage the quality function/s / teams for multiple sites within the group. The QD will be responsible for 5 direct & 40+ indirect reports.
The role:
• Manage the Quality Function across business entities ensuring Compliance status is maintained in support of business strategy
• Provide assistance to all functions within the business on technical and regulatory matters to ensure changing regulatory landscapes are accommodated in support of business objectives
• To lead, motivate and develop the quality teams in support of business plans and profitability goals
• Performing duties as required by a Pharmaceutical Qualified Person under pertinent regulations
• Ensure delivery of quality oversight in in-house and external third-party manufacturing operations
• Provide guidance to Sales and Marketing teams engaged in UK and Export territories as appropriate
• Liaise with and undertake the role of principle point of contact for UK MHRA and UK Home Office Departments in support of business strategy
• To promote and adhere to Health, Safety and Environmental regulations to ensure the wellbeing of the company's employees, contractors and visitors in compliance with legislative requirements.
• To act as a pharmaceutical qualified person to certify products as suitable for release to market
The Person:
• QP qualification essential
• Significant experience working as in a senior quality role within solid dose and none - sterile liquid pharmaceutical settings working and implementing QMS strategies.
• Significant experience working with cGxP regulations
• Previous management/ supervisory experience in a quality setting
Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or GDPR please get in touch with us here.
- Type:
- Permanent
- Start Date:
- 23/04/2024
- Contract Length:
- N/A
- Contact Name:
- Login or register to view
- Job Reference:
- J91978564
- Job ID:
- 221532027
- Applications:
- Less than 10
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